- Domino 1,3-dipolar cycloadditions of N-alkyl-α-amino esters with paraformaldehyde: a direct access to α-hydroxymethyl α-amino acidsCastello, Luis M.; et al, Synthesis, 2014, 46(7), 967-971
Cas no 915405-01-5 (D-Serine, N-methyl-)
D-Serine, N-methyl- structure
Product Name:D-Serine, N-methyl-
CAS No:915405-01-5
MF:C4H9NO3
MW:119.119161367416
CID:787089
PubChem ID:5288119
Update Time:2024-10-26
D-Serine, N-methyl- Chemical and Physical Properties
Names and Identifiers
-
- D-Serine, N-methyl-
- (2R)-3-hydroxy-2-(methylamino)propanoic acid
- N-METHYL-D-SERINE HYDROCHLORIDE
- N-Methyl-D-serine (ACI)
- (R)-3-Hydroxy-2-(methylamino)propanoicacid
- Q27459725
- F11106
- SCHEMBL170982
- CS-0151242
- BS-50942
- (R)-3-Hydroxy-2-(methylamino)propanoic acid
- N-METHYL-D-SERINE
- MFCD19220663
- 915405-01-5
- DTXSID80415335
-
- Inchi： 1S/C4H9NO3/c1-5-3(2-6)4(7)8/h3,5-6H,2H2,1H3,(H,7,8)/t3-/m1/s1
- InChI Key： PSFABYLDRXJYID-GSVOUGTGSA-N
- SMILES： [C@@H](NC)(CO)C(=O)O
Computed Properties
- Exact Mass: 119.058243149g/mol
- Monoisotopic Mass: 119.058243149g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 3
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 8
- Rotatable Bond Count: 3
- Complexity: 83.4
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 1
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: -2.9
- Topological Polar Surface Area: 69.6?2
Experimental Properties
- Density: 1.242
D-Serine, N-methyl- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-XH960-200mg |
D-Serine, N-methyl- |
915405-01-5 | 97% | 200mg |
1275.0CNY | 2021-07-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-XH960-50mg |
D-Serine, N-methyl- |
915405-01-5 | 97% | 50mg |
511.0CNY | 2021-07-10 | |
| Ambeed | A667309-100mg |
(R)-3-Hydroxy-2-(methylamino)propanoic acid |
915405-01-5 | 97% | 100mg |
$64.0 | 2025-04-15 | |
| Ambeed | A667309-250mg |
(R)-3-Hydroxy-2-(methylamino)propanoic acid |
915405-01-5 | 97% | 250mg |
$103.0 | 2025-04-15 | |
| Ambeed | A667309-1g |
(R)-3-Hydroxy-2-(methylamino)propanoic acid |
915405-01-5 | 97% | 1g |
$278.0 | 2025-04-15 | |
| Chemenu | CM541349-100mg |
(R)-3-Hydroxy-2-(methylamino)propanoic acid |
915405-01-5 | 95%+ | 100mg |
$120 | 2024-07-20 | |
| Chemenu | CM541349-250mg |
(R)-3-Hydroxy-2-(methylamino)propanoic acid |
915405-01-5 | 95%+ | 250mg |
$181 | 2024-07-20 | |
| Chemenu | CM541349-1g |
(R)-3-Hydroxy-2-(methylamino)propanoic acid |
915405-01-5 | 95%+ | 1g |
$452 | 2024-07-20 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X17635-100mg |
(R)-3-Hydroxy-2-(methylamino)propanoic acid |
915405-01-5 | 97% | 100mg |
￥376.0 | 2024-07-18 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X17635-1g |
(R)-3-Hydroxy-2-(methylamino)propanoic acid |
915405-01-5 | 97% | 1g |
￥1691.0 | 2024-07-18 |
D-Serine, N-methyl- Production Method
Production Method 1
Reaction Conditions
1.1 Reagents: Dicyclohexylcarbodiimide Solvents: Dichloromethane ; 10 min, 25 °C
1.2 Reagents: (1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenylethyl)cyclohexanol ; 25 °C; 24 h, 25 °C
1.3 Reagents: Trifluoroacetic acid Solvents: Dichloromethane
1.4 Reagents: Triethylamine ; 1 h, 110 °C
1.5 Reagents: Hydrochloric acid Solvents: Ethanol , Water ; 24 h, 78 °C
1.6 Reagents: (±)-Propylene oxide Solvents: Ethanol ; 30 min, 78 °C
1.2 Reagents: (1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenylethyl)cyclohexanol ; 25 °C; 24 h, 25 °C
1.3 Reagents: Trifluoroacetic acid Solvents: Dichloromethane
1.4 Reagents: Triethylamine ; 1 h, 110 °C
1.5 Reagents: Hydrochloric acid Solvents: Ethanol , Water ; 24 h, 78 °C
1.6 Reagents: (±)-Propylene oxide Solvents: Ethanol ; 30 min, 78 °C
Reference
Production Method 2
Reaction Conditions
1.1 Reagents: Triethylamine ; 1 h, 110 °C
2.1 Reagents: Hydrochloric acid Solvents: Ethanol , Water ; 24 h, 78 °C
2.2 Reagents: (±)-Propylene oxide Solvents: Ethanol ; 30 min, 78 °C
2.1 Reagents: Hydrochloric acid Solvents: Ethanol , Water ; 24 h, 78 °C
2.2 Reagents: (±)-Propylene oxide Solvents: Ethanol ; 30 min, 78 °C
Reference
- Domino 1,3-dipolar cycloadditions of N-alkyl-α-amino esters with paraformaldehyde: a direct access to α-hydroxymethyl α-amino acidsCastello, Luis M.; et al, Synthesis, 2014, 46(7), 967-971
Production Method 3
Reaction Conditions
1.1 Reagents: Dicyclohexylcarbodiimide Solvents: Dichloromethane ; 10 min, 25 °C
1.2 25 °C; 24 h, 25 °C
1.3 Reagents: Trifluoroacetic acid Solvents: Dichloromethane
2.1 Reagents: Triethylamine ; 1 h, 110 °C
3.1 Reagents: Hydrochloric acid Solvents: Ethanol , Water ; 24 h, 78 °C
3.2 Reagents: (±)-Propylene oxide Solvents: Ethanol ; 30 min, 78 °C
1.2 25 °C; 24 h, 25 °C
1.3 Reagents: Trifluoroacetic acid Solvents: Dichloromethane
2.1 Reagents: Triethylamine ; 1 h, 110 °C
3.1 Reagents: Hydrochloric acid Solvents: Ethanol , Water ; 24 h, 78 °C
3.2 Reagents: (±)-Propylene oxide Solvents: Ethanol ; 30 min, 78 °C
Reference
- Domino 1,3-dipolar cycloadditions of N-alkyl-α-amino esters with paraformaldehyde: a direct access to α-hydroxymethyl α-amino acidsCastello, Luis M.; et al, Synthesis, 2014, 46(7), 967-971
Production Method 4
Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Ethanol , Water ; 24 h, 78 °C
1.2 Reagents: (±)-Propylene oxide Solvents: Ethanol ; 30 min, 78 °C
1.2 Reagents: (±)-Propylene oxide Solvents: Ethanol ; 30 min, 78 °C
Reference
- Domino 1,3-dipolar cycloadditions of N-alkyl-α-amino esters with paraformaldehyde: a direct access to α-hydroxymethyl α-amino acidsCastello, Luis M.; et al, Synthesis, 2014, 46(7), 967-971
Production Method 5
Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Ethanol , Water ; 24 h, 78 °C
1.2 Reagents: (±)-Propylene oxide Solvents: Ethanol ; 30 min, 78 °C
1.2 Reagents: (±)-Propylene oxide Solvents: Ethanol ; 30 min, 78 °C
Reference
- Domino 1,3-dipolar cycloadditions of N-alkyl-α-amino esters with paraformaldehyde: a direct access to α-hydroxymethyl α-amino acidsCastello, Luis M.; et al, Synthesis, 2014, 46(7), 967-971
Production Method 6
Reaction Conditions
1.1 Reagents: Triethylamine ; 1 h, 110 °C
2.1 Reagents: Hydrochloric acid Solvents: Ethanol , Water ; 24 h, 78 °C
2.2 Reagents: (±)-Propylene oxide Solvents: Ethanol ; 30 min, 78 °C
2.1 Reagents: Hydrochloric acid Solvents: Ethanol , Water ; 24 h, 78 °C
2.2 Reagents: (±)-Propylene oxide Solvents: Ethanol ; 30 min, 78 °C
Reference
- Domino 1,3-dipolar cycloadditions of N-alkyl-α-amino esters with paraformaldehyde: a direct access to α-hydroxymethyl α-amino acidsCastello, Luis M.; et al, Synthesis, 2014, 46(7), 967-971
Production Method 7
Reaction Conditions
1.1 Reagents: Dicyclohexylcarbodiimide Solvents: Dichloromethane ; 10 min, 25 °C; 25 °C; 24 h, 25 °C
1.2 25 °C; 24 h, 25 °C
1.3 Reagents: Trifluoroacetic acid Solvents: Dichloromethane
2.1 Reagents: Triethylamine ; 1 h, 110 °C
3.1 Reagents: Hydrochloric acid Solvents: Ethanol , Water ; 24 h, 78 °C
3.2 Reagents: (±)-Propylene oxide Solvents: Ethanol ; 30 min, 78 °C
1.2 25 °C; 24 h, 25 °C
1.3 Reagents: Trifluoroacetic acid Solvents: Dichloromethane
2.1 Reagents: Triethylamine ; 1 h, 110 °C
3.1 Reagents: Hydrochloric acid Solvents: Ethanol , Water ; 24 h, 78 °C
3.2 Reagents: (±)-Propylene oxide Solvents: Ethanol ; 30 min, 78 °C
Reference
- Domino 1,3-dipolar cycloadditions of N-alkyl-α-amino esters with paraformaldehyde: a direct access to α-hydroxymethyl α-amino acidsCastello, Luis M.; et al, Synthesis, 2014, 46(7), 967-971
D-Serine, N-methyl- Raw materials
- L(-)-Menthol
- Boc-Sar-OH
- (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)cyclohexanol
- (1R,2S,5R)-5-Methyl-2-(1-methylethyl)cyclohexyl (4R)-3-methyl-4-oxazolidinecarboxylate
- (1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenylethyl)cyclohexyl (4R)-3-methyl-4-oxazolidinecarboxylate
- Glycine, N-methyl-, (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl ester
- 4-Oxazolidinecarboxylic acid, 3-methyl-, (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl ester, (4S)-
- (1R,2S,5R)-5-Methyl-2-(1-methyl-1-phenylethyl)cyclohexyl (4S)-3-methyl-4-oxazolidinecarboxylate
- Glycine, N-methyl-, (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenylethyl)cyclohexyl ester
D-Serine, N-methyl- Preparation Products
D-Serine, N-methyl- Suppliers
Amadis Chemical Company Limited
Gold Member
Audited Supplier
(CAS:915405-01-5)D-Serine, N-methyl-
Order Number:A900795
Stock Status:in Stock
Quantity:1g/5g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 12:06
Price ($):228.0/797.0
Email:[email protected]
D-Serine, N-methyl- Related Literature
-
Joo Chuan Yeo,Kenry Lab Chip, 2016,16, 4082-4090
-
Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
-
Chao-Han Cheng,Wen-Zhen Wang,Shie-Ming Peng,I-Chia Chen Phys. Chem. Chem. Phys., 2017,19, 25471-25477
-
Qiao Song,Angela Bamesberger,Lingyun Yang,Haley Houtwed,Haishi Cao Analyst, 2014,139, 3588-3592
-
Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
915405-01-5 (D-Serine, N-methyl-) Related Products
- 3913-67-5(H-N-Me-Ala-OH)
- 2812-34-2(L-Serine, N,N-dimethyl-)
- 126576-99-6((2R)-2-(dimethylamino)-3-hydroxypropanoic acid)
- 777836-89-2(Serine,N-(carboxymethyl)-)
- 17136-47-9(L-Serine,N-(carboxymethyl)-)
- 2480-26-4(H-N-Me-Ser-OH)
- 28413-45-8(L-Alanine, N-methyl-,potassium salt (1:1))
- 600-21-5(H-N-Me-DL-Ala-OH)
- 29475-64-7(N-Methyl-D-alanine)
- 83293-50-9(L-Serine, N-ethyl-)
Recommended suppliers
Amadis Chemical Company Limited
(CAS:915405-01-5)D-Serine, N-methyl-
Purity:99%/99%
Quantity:1g/5g
Price ($):228.0/797.0